510(k) K020794

SALICYLATE ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM by Bayer Diagnostics Corp. — Product Code DKJ

K020794 is an FDA 510(k) premarket notification submitted by Bayer Diagnostics Corp. for the device "SALICYLATE ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM". The FDA issued a decision of Substantially Equivalent on July 11, 2002. The device falls under product code DKJ (Colorimetry, Salicylate), a Class II device regulated under 21 CFR 862.3830. Bayer Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 11, 2002
Date Received
March 11, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimetry, Salicylate
Device Class
Class II
Regulation Number
862.3830
Review Panel
TX
Submission Type